Volume 48, Issue 1 pp. 28-34
Research Article

Prevention and monitoring of invasive fungal infections in pediatric patients with cancer and hematologic disorders

Liisa Hovi MD

Corresponding Author

Liisa Hovi MD

Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland

Hospital for Children and Adolescents, P.O. Box 281, University of Helsinki, 00029 HUS, Finland.===Search for more papers by this author
Harri Saxen MD

Harri Saxen MD

Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland

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Ulla M. Saarinen-Pihkala MD

Ulla M. Saarinen-Pihkala MD

Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland

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Kim Vettenranta MD

Kim Vettenranta MD

Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland

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Taru Meri MSc

Taru Meri MSc

Department of Bacteriology & Immunology, University of Helsinki, Helsinki, Finland

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Malcolm Richardson PhD

Malcolm Richardson PhD

Department of Bacteriology & Immunology, University of Helsinki, Helsinki, Finland

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First published: 04 January 2006
Citations: 57

Abstract

Background

The occurrence of invasive fungal infection (IFIs) in a pediatric hematology/oncology unit after renovation of the ventilation system, and initiating routine azole antifungal prophylaxis was monitored. In addition, the value of serial screening for Aspergillus galactomannan (GM) for diagnosing invasive aspergillosis was assessed.

Procedure

A total of 98 consecutive high-risk pediatric patients were prospectively surveyed for signs of IFI and weekly monitored for serum GM. The data was not made available to treating physicians.

Results

Only 2 patients had proven and 27 possible IFI based on the European Organization for Research and Treatment of Cancer/Mycoses Study Group definitions. The incidence of proven IFI was 1/31 (3.2%) in the allogeneic stem cell transplant (SCT) (Aspergillus spp), 0/26 in the autologous SCT, and 1/60 (1.6%) in the induction therapy group (C. krusei). GM was detected at least in one tested sample in 12/98 patients (12.2%), in five patients in two or more sequential samples. In the latter group, IFI was proven in one patient and could not be excluded in the others. Four of the five patients belonged to the 31 allogeneic and one to the 26 autologous SCT patients. In patients with only one positive GM test none developed signs of IFI and only one received empirical amphotericin B.

Conclusions

With the currently used preventative and prophylactic measures, IFI is uncommon in children with high-risk for infection. Regular screening for GM could be useful among allogeneic SCT patients and two positive samples should prompt further investigative procedures and pre-emptive antifungal therapy. Pediatr Blood Cancer 2007;48:28–34. © 2006 Wiley-Liss, Inc.

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